Allele Registry

Canonical Allele Identifier: PA2827326231

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000674965

ClinVar Variation:

558661

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317507.1:p.Gly865Cys	CA388033415 NM_001330578.2:c.2593G>T